Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility

Background: Semaphorin-3A (Sema3A) and Semaphorin-7A (Sema7A) play crucial roles in immune system by inhibiting T cell proliferation and leading to the secretion of pro-inflammatory cytokines. Increasing evidence suggest that Sema3A and Sema7A may link to the development and pathogenesis of systemic...

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Main Authors: Li-Na Liu, Peng Wang, Yan-Feng Zou, Zhiwei Xu, Jian Cheng, Yuzhou Zhang, Wenbiao Hu, Hai-Feng Pan
Format: Article
Language:English
Published: Taylor & Francis Group 2019-05-01
Series:Autoimmunity
Subjects:
Online Access:http://dx.doi.org/10.1080/08916934.2019.1642333
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author Li-Na Liu
Peng Wang
Yan-Feng Zou
Zhiwei Xu
Jian Cheng
Yuzhou Zhang
Wenbiao Hu
Hai-Feng Pan
author_facet Li-Na Liu
Peng Wang
Yan-Feng Zou
Zhiwei Xu
Jian Cheng
Yuzhou Zhang
Wenbiao Hu
Hai-Feng Pan
author_sort Li-Na Liu
collection DOAJ
description Background: Semaphorin-3A (Sema3A) and Semaphorin-7A (Sema7A) play crucial roles in immune system by inhibiting T cell proliferation and leading to the secretion of pro-inflammatory cytokines. Increasing evidence suggest that Sema3A and Sema7A may link to the development and pathogenesis of systemic lupus erythematosus (SLE). Objective: This study aims to evaluate the association of Sema3A, Sema7A gene single-nucleotide polymorphisms (SNPs) with susceptibility to SLE. Methods: There were 495 SLE patients and 493 healthy controls in the study. Sema3A gene and Sema7A gene were genotyped by improved multiple ligase detection reaction (iMLDR), their plasma expression levels were detected by enzyme-linked immunosorbent assay (ELISA). Results: No differences in genotype and allele frequencies of these SNPs were observed between SLE patients and healthy controls. However, analysing Sema3A and Sema7A SNPs with clinical manifestations of SLE indicated that, in Sema3A, the A allele frequencies of rs7804122 polymorphism was higher in patients with oral ulcers. In Sema7A, there were differences in allele frequencies of the rs2075589 and rs28362930 polymorphisms between SLE patients with haematological disorder and those without. The GG genotype and G allele frequencies of rs28362930 and the CC genotype, and C allele frequencies of rs741761 were both related to discoid rash in SLE patients. The allele frequency of G (rs28362930) was higher in SLE patients with renal disorder. There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. No differences in plasma Sema3A and Sema7A levels were detected in SLE patients of different genotypes. Conclusions: Sema3A and Sema7A gene polymorphisms are not related to SLE genetic susceptibility, but may link to several clinical features of SLE.
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spelling doaj.art-5d4f1e8a97484b9bb86f3ef4aac4ede32023-09-15T10:01:08ZengTaylor & Francis GroupAutoimmunity0891-69341607-842X2019-05-0152416116710.1080/08916934.2019.16423331642333Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibilityLi-Na Liu0Peng Wang1Yan-Feng Zou2Zhiwei Xu3Jian Cheng4Yuzhou Zhang5Wenbiao Hu6Hai-Feng Pan7Anhui Medical UniversityMedical College of Soochow UniversityAnhui Medical UniversityQueensland University of TechnologyQueensland University of TechnologyQueensland University of TechnologyQueensland University of TechnologyAnhui Medical UniversityBackground: Semaphorin-3A (Sema3A) and Semaphorin-7A (Sema7A) play crucial roles in immune system by inhibiting T cell proliferation and leading to the secretion of pro-inflammatory cytokines. Increasing evidence suggest that Sema3A and Sema7A may link to the development and pathogenesis of systemic lupus erythematosus (SLE). Objective: This study aims to evaluate the association of Sema3A, Sema7A gene single-nucleotide polymorphisms (SNPs) with susceptibility to SLE. Methods: There were 495 SLE patients and 493 healthy controls in the study. Sema3A gene and Sema7A gene were genotyped by improved multiple ligase detection reaction (iMLDR), their plasma expression levels were detected by enzyme-linked immunosorbent assay (ELISA). Results: No differences in genotype and allele frequencies of these SNPs were observed between SLE patients and healthy controls. However, analysing Sema3A and Sema7A SNPs with clinical manifestations of SLE indicated that, in Sema3A, the A allele frequencies of rs7804122 polymorphism was higher in patients with oral ulcers. In Sema7A, there were differences in allele frequencies of the rs2075589 and rs28362930 polymorphisms between SLE patients with haematological disorder and those without. The GG genotype and G allele frequencies of rs28362930 and the CC genotype, and C allele frequencies of rs741761 were both related to discoid rash in SLE patients. The allele frequency of G (rs28362930) was higher in SLE patients with renal disorder. There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. No differences in plasma Sema3A and Sema7A levels were detected in SLE patients of different genotypes. Conclusions: Sema3A and Sema7A gene polymorphisms are not related to SLE genetic susceptibility, but may link to several clinical features of SLE.http://dx.doi.org/10.1080/08916934.2019.1642333semaphorin-3asemaphorin-7asingle-nucleotide polymorphismssystemic lupus erythematosus
spellingShingle Li-Na Liu
Peng Wang
Yan-Feng Zou
Zhiwei Xu
Jian Cheng
Yuzhou Zhang
Wenbiao Hu
Hai-Feng Pan
Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
Autoimmunity
semaphorin-3a
semaphorin-7a
single-nucleotide polymorphisms
systemic lupus erythematosus
title Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
title_full Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
title_fullStr Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
title_full_unstemmed Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
title_short Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility
title_sort semaphorin 3a semaphorin 7a gene single nucleotide polymorphisms and systemic lupus erythematosus susceptibility
topic semaphorin-3a
semaphorin-7a
single-nucleotide polymorphisms
systemic lupus erythematosus
url http://dx.doi.org/10.1080/08916934.2019.1642333
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